Shoot, Stolon, and Tuber Formation on Potato (Solanum tuberosum L.) Cuttings in Response to Photoperiod

The intensity of “tuberization stimulus” in potato shoots (Solanum tuberosum L.) can be assessed from cuttings containing one or more leaves. Cuttings maintained in a mist chamber under long days will form tubers from underground buds if prior to taking the cutting the leaves received sufficient exposure to photoperiods less than the critical photoperiod. The greatest tendency to tuberize was found in cuttings that consisted of a single, fully expanded leaf and its subtended bud. Grafts showed that genetical differences in critical photoperiod resided in properties of the leaf. Short days before cutting tended to shift growth from above ground buds of two-node cuttings to below ground buds, even if the number of short days was insufficient for tuber induction. As few as 6 short days reduced growth of shoots at the upper bud and increased underground growth of shoots and stolons.     

DEVELOPMENTAL POTENTIAL OF AXILLARY BUDS OF WATER HYACINTH,EICHHORNIA CRASSIPES SOLMS. (PONTEDERIACEAE)

Buds axillary to foliage leaves of water hyacinth can elongate either as vegetative stolons or as renewal shoots produced in association with the terminal inflorescence. Stolons differ from renewal shoots in position within the shoot system, morphology, and function. Renewal shoot buds always expand, whereas stolon buds may or may not. A stolon bud develops in conjunction with the subtending leaf; as that leaf matures, the stolon bud reaches a critical period in development. At this point, the bud either continues to expand, producing a stolon, or it stops growth and matures. Maturation is not irreversible, but the probability of a bud expanding decreases as bud age increases. In the field, buds on plants at the water hyacinth mat edge frequently produce stolons, whereas buds on plants inside the mat rarely do so. Leaf morphology also varies between plants in these two regions of the mat. The particular association of leaf and branch type found in the field, however, can be reversed experimentally, indicating that although leaf and bud development are coordinated, the particular course of each is independent.     

Effects of growth regulators, CCC and B9, on some potato varieties

The effects of CCC and B 9 on the growth habit of potato differed between varieties. CCC diminished stem lengths and dry weight more than Bo because CCC was applied early when shoots emerged from the soil, but B 9 was applied about 3 weeks later when several leaves had formed. In some varieties lateral stem growth was increased by treatment and in others decreased. There was an inverse relation between main stem and lateral stem growth so that varieties with vigorous main stem growth had poor lateral growth and vice-versa. Treatment with the growth-regulators diminished leaf dry weight of main stem leaves less than leaf area, but the degree of magnitudes of the changes depended on the variety. Both regulators lessened net assimilation rate. Net assimilation rate and dry matter per unit area of leaf were inversely related, possibly because accumulation of substances in leaves decreases photosynthesis. Stolon dry weight was positively correlated with main stem leaf area. There was a direct relation between stem length and tuber dry weight, suggesting that tuber initiation occurs at different stem lengths in different varieties. Tubering was earliest in Epicure and latest in King Edward. Epicure had the greatest tuber weight and smallest stem length.     

Stem canker (Rhizoctonia solani) on five early and seven maincrop potato cultivars I. Infection of shoots, stolons and tubers

In 1983 and 1984, potato seed tubers of five early and seven maincrop cultivars were inoculated with cultures of Rhizoctonia soluni during planting to simulate severe seed infection. Shoot and stolon infection was assessed in June-August and black scurf on tubers recorded after harvest in October. Almost all shoots of all cultivars had stem canker in both years and disease on shoots, stolons and tubers was more severe in 1984 than in 1983. In 1983 similar amounts of disease developed on all early cultivars and between 11% (Ulster Sceptre) and 32% (Maris Peer) shoots were pruned off. Maris Peer had a stem canker score lower than other cultivars in 1984 but more than half the shoots were pruned off. Shoot pruning on Estima, Ulster Prince and Ulster Sceptre was more common on plants from sprouted than non-sprouted seed. Between 30 and 50% of stolons were pruned off. After harvest in 1985, black scurf was least prevalent on Arran Comet and Maris Peer tubers and in 1984 on Arran Comet and Estima tubers from non-sprouted seed. Of the maincrop cultivars, King Edward plants from sprouted seed had many shoots pruned off in both years. Shoot pruning was also prevalent on Maris Piper and Pentland Squire plants from non-sprouted seed. Record had fewest pruned shoots and stolons and the lowest stem canker score. The disease was more severe on Pentland Crown and Maris Piper plants from non-sprouted than sprouted seed. Black scurf was most common on Cara and King Edward tubers in 1983 and on King Edward and Record tubers in 1984. In both years few shoots but many tubers were infected on plants from non-inoculated seed and the significance of this is discussed.     

AXR1 acts after lateral bud formation to inhibit lateral bud growth in Arabidopsis

The AXR1 gene of Arabidopsis is required for many auxin responses. The highly branched shoot phenotype of mature axr1 mutant plants has been taken as genetic evidence for a role of auxin in the control of shoot branching. We compared the development of lateral shoots in wild-type Columbia and axr1-12 plants. In the wild type, the pattern of lateral shoot development depends on the developmental stage of the plant. During prolonged vegetative growth, axillary shoots arise and develop in a basal-apical sequence. After floral transition, axillary shoots arise rapidly along the primary shoot axis and grow out to form lateral inflorescences in an apical-basal sequence. For both patterns, the axr1 mutation does not affect the timing of axillary meristem formation; however, subsequent lateral shoot development proceeds more rapidly in axr1 plants. The outgrowth of lateral inflorescences from excised cauline nodes of wild-type plants is inhibited by apical auxin. axr1-12 nodes are resistant to this inhibition. These results provide evidence for common control of axillary growth in both patterns, and suggest a role for auxin during the late stages of axillary shoot development following the formation of the axillary bud and several axillary leaf primordia.     

THE TENDRIL OF PARTHENOCISSUS INSERTA: DETERMINATION AND DEVELOPMENT

Tendrils on long shoots of Parthenocissus inserta occur in a regular pattern opposite the alternate distichous leaves at two successive nodes of each three nodes. Ontogenetic study shows that the tendril is initiated at the flank of the shoot apex during the second plastochron in an essentially axillary position. It is carried upward with growth of the internode above the axillant leaf and ultimately is situated opposite the next younger leaf. In a rhythmic pattern a different group of appendages is produced by the shoot apex at each node in the sequence of three. In acropetal order these are: at the tendrilless node the leaf subtends an axillary bud complex which in turn subtends a tendril; the leaf at the lower tendril-bearing node directly subtends a tendril, and the leaf at the upper tendril-bearing node subtends an axillary bud. Tendril primordia were not induced to develop as foliaceous shoots when cultured in vitro or in decapitation experiments, indicating that the meristem which becomes a tendril is determined early in its inception. Although built on a shoot pattern, the tendril is regarded as an organ sui generis with a possible relationship to the inflorescence. The morphological nature of the tendril is discussed in the light of theories postulated in the literature.     

Growth forms of Leymus chinesis (Poaceae) at the different developmental stages of the natural population

The manner in which the density of Leymus chinensis increases from a single plant to a dominant population can be understood by tracing the development of a population from early to late stages. Parent shoot density, above‐ground dry weight, spike density, heading rate and spike dry weight, density of spreading shoots (buds/daughter shoots in apical/axillary rhizomes) and clumping shoots (buds/daughter shoots in axillary parent shoots), and young rhizome length and weight were investigated in the same quadrats for a low density/early stage (LE) population and a high density/late stage (HL) population. Clonal growth (buds/daughter shoots formation) and sexual reproduction (spikes formation) increased while rhizome storage (young rhizome weight) decreased during the transition from LE to HL. In a LE population an outward occupation strategy was employed, with a high proportion of spreading shoots. As the population density gradually increased until HL, an inward consolidation strategy increasing shoot amount in previously occupied areas, was adopted. This was characterized by a high proportion of clumping shoots. Interestingly, the trade‐off between spreading and clumping shoots can be adjusted by the duration of young rhizome elongation during a growth season. In other words, compared with a HL population, a LE population shortened the duration of young rhizome elongation during the growth season, which resulted in more time for the production of axillary spreading shoots along the rhizomes, and high amounts and proportions of total spreading shoots. The special growth patterns, that is, trade‐offs among growth forms, allow L. chinensis to establish dominant populations throughout the eastern Eurasian Steppe.     

Factors affecting the detection of potato leafroll virus in potato foliage by enzyme-linked immunosorbent assay

Using antiserum globulins that reacted only weakly with plant materials, potato leafroll virus (PLRV) at 10 ng/ml was detected consistently by enzyme-linked immunosorbent assay (ELISA). The reaction with PLRV particles was slightly impaired in potato leaf extracts that were diluted less than 10^-1 but not at greater dilutions. Antiserum globulins that reacted more strongly with plant materials could be used satisfactorily for coating microtitre plates but were unsuitable for conjugating with enzyme. The detection end-point of PLRV, in leaf sap of potato cv. Cara plants grown from infected tubers in the glasshouse, was about 10^-2 and the virus was reliably detected in extracts of composite samples of one infected and 15 virus-free leaves. PLRV concentration was much less in extracts of roots or stolons than in leaf extracts. The virus was detected in infected leaves of all 27 cultivars tested. PLRV was readily detectable 2 wk before symptoms of secondary infection developed in field-grown plants of cv. Cara and Maris Piper and remained so for at least 5 wk. Its concentration was slightly greater in old than in young leaves and was similar to that in glasshouse-grown plants. In field-grown plants of cv. Maris Piper with primary infection, PLRV was detected in tip leaves 21–42 days after lower leaves were inoculated by aphids; in some shoots it later reached a concentration, in tip leaves, similar to that in leaves with secondary infection. Symptoms of primary infection developed in the young leaves of some infected shoots but were inconspicuous and were not observed until at least a week after PLRV was detected by ELISA.     

Development of shoot inHydrangea macrophylla II. sequence and timing

The development of axillary buds, terminal buds, and the shoots extended from them was studied inHydrangea macrophylla. The upper and lower parts in a nonflower-bearing shoot are discernible; the preformed part of a shoot develops into the lower part and the neoformed part into the upper part (Zhou and Hare, 1988). These two part are formed by the different degrees of internode elongation at early and late phases during a growth season, respectively. Leaf pairs in the neoformed part of the shoot are initiated successively with a plastochron of 5–20 days after the bud burst in spring. The upper axillary buds are initiated at approximately the same intervals as those of leaf pairs, but 10–30 days later than their subtending leaves. Changes in numbers of leaf pairs and in lengths of successive axillary buds show a pattern similar to the changes in internode lengths of the shoot at the mature stage. The uppermost axillary buds of the flower-bearing shoot often begin extending into new lateral shoots when the flowering phase has ended. The secondary buds in terminal and lower axillary buds are initiated and developed in succession during the late phase of the growth season. Internode elongation seems to be important in determining the degrees of development of the axillary buds. Pattern of shoot elongation is suggested to be relatively primitive. Significances of apical dominance and environmental conditions to shoot development are discussed.     

Suppression of a vegetative MADS box gene of potato activates axillary meristem development

Potato MADS box 1 (POTM1) is a member of the SQUAMOSA-like family of plant MADS box genes isolated from an early stage tuber cDNA library. The RNA of POTM1 is most abundant in vegetative meristems of potato (Solanum tuberosum), accumulating specifically in the tunica and corpus layers of the meristem, the procambium, the lamina of new leaves, and newly formed axillary meristems. Transgenic lines with reduced levels of POTM1 mRNA exhibited decreased apical dominance accompanied by a compact growth habit and a reduction in leaf size. Suppression lines produced truncated shoot clusters from stem buds and, in a model system, exhibited enhanced axillary bud growth instead of producing a tuber. This enhanced axillary bud growth was not the result of increased axillary bud formation. Tuber yields were reduced and rooting of cuttings was strongly inhibited in POTM1 suppression lines. Both starch accumulation and the activation of cell division occurred in specific regions of the vegetative meristems of the POTM1 transgenic lines. Cytokinin levels in axillary buds of a transgenic suppression line increased 2- to 3-fold. These results imply that POTM1 mediates the control of axillary bud development by regulating cell growth in vegetative meristems.     

Cell Cycling and the Fate of Potato Buds

The cell cycling characteristics of the regions of the apicalmeristems of underground shoots and buds of Solanum tuberosumL. were investigated by stathmokinesis and labelling. The apicaldomes of orthotropic shoots produce cells at twice the elementalrate of those of stolons, and their youngest leaf primordiaat twelve times the rate. Changing the fate of stolons so thatthey will become orthotropic by decapitating the tuber sproutsthat bear them results within 24 h in a general increase incell production especially in the leaf primordia. Axillary buds on tuber sprouts induced to become precursorsof orthotropic shoots instead of stolons undergo a spectacularincrease in cell division within 24 h in all regions, especiallyin the primordia and bud anlagen where the rate increases 20-foldor more. The summit is slower to react than other regions, but,by 24 h, its rate of cell division increases 11-fold and itis contributing 14 cells per day to the flanks from its 80 cells. In all the axillary buds the rate of mitosis in the summit ishalf that of the flanks of the apical dome, but, in both stolonsand orthotropic underground shoots, the rate is higher in thesummit than in the flanks or rib meristem. The results are discussed in relation to what is known of cellcycling changes after floral evocation. Solanum tuberosum L., potato, fate, cell division, apical meristem, stathmokinesis     

Patterns of 14C-labelled Assimilate Partitioning in Red and White Clover During Vegetative Growth

A quantitative analysis of the ¹⁴C-labelled assimilate suppliedby the expanded leaves on the primary shoot to growing leaves,stem, lateral shoots (branches or stolons) and roots in redand white clover was conducted during vegetative growth. Stem growth of the primary shoot was inhibited in both cloversand utilized no energy resources. The growing leaves at theprimary shoot apex of white clover imported 4 per cent of theshoot's assimilate compared with 10 per cent in red clover.At the basal end of the primary shoot, the tap root of whiteclover imported 16 per cent of the shoot's assimilate comparedwith 22 per cent in red clover. Branches in red clover and stolonsin white clover were by far the largest sinks for primary shootassimilate, importing 39 per cent and 63 per cent of the labelledassimilate, respectively. Analyses of the translocation of assimilate from individualprimary shoot leaves demonstrated that in both clovers olderleaves exported more of their assimilate to branches or stolons,whereas younger leaves exported more of their assimilate toroots, and possibly in white clover, to growing leaves at thetip of the shoot. Of the labelled assimilate exported to branchesor stolons, each primary shoot leaf exported preferentiallyto the branch or stolon in its own axil, but in addition exportedsubstantial quantities of assimilate to all other axillary shoots,particularly those arising from basal axils where the subtendingleaf had died. Trifolium repens, Trifolium pratense, red clover, white clover, assimilate partitioning, perennation     

A COMPARATIVE DEVELOPMENTAL STUDY OF THE MUTANT SIDESHOOTLESS AND NORMAL TOMATO PLANTS

'Sideshootless,’ a mutant strain of tomato which does not produce axillary buds during vegetative growth, was compared with normally branching plants in order to study the nature of development particularly with regard to axillary buds. Sectioned material revealed no indication of axillary bud initiation in the sideshootless plant at any time during the vegetative phase of growth. In the normal plants, buds were noted to arise in the axil of the fifth youngest leaf. The buds take their origin in tissue which is in direct continuity with the apical meristem. The bud primordia later become set apart from the apex as vacuolation takes place in the surrounding tissue. At the time of floral initiation, the mutant and normal strains behave similarly. Axillary buds appear in the axils of the 2 leaves immediately below the floral apex. One of the buds elongates to overtop the existing plant axis; the other develops as a typical sidebranch. The inflorescence is pushed aside in the process. This pattern is repeated with each inflorescence; thus an axis composed of several superimposed laterals results.     

Studies on the growth and development of Oxalis latifolia

The growth and development of Oxalis latifolia was assessed on outdoor-grown potted plants raised from bulbs. Three main phases of growth appeared to be correlated with major physiological developments in the aerial and subterranean organs. Establishment (weeks 1 – 5) was characterised by a slow gain in plant dry weight accompanied by high relative growth rate (RGR) values for individual plant organs. The second phase of growth (weeks 6 – 12) was reproductive, as stolons grew and initiated bulbils at the apices. Bulbils had the capacity to produce their own shoot system and ultimately some primary bulbils supported secondary bulbils. Dry matter accumulation was in the order: bulbils > peduncles > leaves > petioles > stolons = roots > parent bulb. The RGR of individual plant organs declined together with the net assimilation (NAR) rates and the leaf area ratio of the shoots during the reproductive phase and beyond into the senescence phase (week 13 onwards). The results are discussed in relation to the problem of achieving weed control via cultural and herbicide treatments.     

BACTERIAL CANKER OF STONE-FRUITS: IV. INVESTIGATION OF A METHOD FOR MEASURING THE INOCULUM POTENTIAL OF CHERRY TREES

Pseudomonas mors-prunorum Wormald, the organism causing bacterial canker of stone-fruits, was present on healthy cherry leaves during the autumn in numbers sufficient to suggest that they were the main source of inoculum for the infection of stems and branches. Quantitative estimates of the pathogen could be obtained by shaking leaves in water and plating out the washings. This method was examined in detail as a possible means of comparing the inoculum potentials on different cherry varieties.
The numbers of the pathogen varied considerably between leaves and between branches, but not between trees of the same variety. It was estimated that a sample of 192 leaves, eight from each of twenty-four different branches would be adequate to show differences between varieties if sufficiently replicated in time. The accuracy of a twenty-four branch sample was tested by comparing parallel samples from two separate groups of trees of the same variety. There was a highly significant correlation between the numbers of bacteria obtained from the two series of samples. From the error variance in an analysis of variance, it was calculated that five successive samples would show a significant difference between two such groups of trees if one exceeded the other by 54%.
It was necessary to wash leaves for 4 hr. or more, depending on temperature, to recover all the bacteria from the leaf surfaces. At temperatures lower than 27° C. however, bacterial growth intervened before this stage was reached. At laboratory temperatures a period of 4 hr. washing was found to be most suitable for comparing varieties and gave 80–90% recovery of bacteria without errors due to growth.
A characteristic flora of non-parasitic bacteria was observed on cherry trees, coexisting with the pathogen on the leaf surfaces. The fungus Pullaria pullulans was also extremely abundant.     

Development and Growth Potential of Axillary Buds in Roses as Affected by Bud Age

The effect of axillary bud age on the development and potentialfor growth of the bud into a shoot was studied in roses. Ageof the buds occupying a similar position on the plant variedfrom 'subtending leaf just unfolded' up to 1 year later. Withincreasing age of the axillary bud its dry mass, dry-matterpercentage and number of leaves, including leaf primordia, increased.The apical meristem of the axillary bud remained vegetativeas long as subjected to apical dominance, even for 1 year. The potential for growth of buds was studied either by pruningthe parent shoot above the bud, by grafting the bud or by culturingthe bud in vitro. When the correlative inhibition (i.e. dominationof the apical region over the axillary buds) was released, additionalleaves and eventually a flower formed. The number of additionalleaves decreased with increasing bud age and became more orless constant for axillary buds of shoots beyond the harvestablestage, while the total number of leaves preceding the flowerincreased. An increase in bud age was reflected in a greaternumber of scales, including transitional leaves, and in a greaternumber of non-elongated internodes of the subsequent shoot.Time until bud break slightly decreased with increasing budage; it was long, relatively, for 1 year old buds, when theysprouted attached to the parent shoot. Shoot length, mass andleaf area were not clearly affected by the age of the bud thatdeveloped into the shoot. With increasing bud age the numberof pith cells in the subsequent shoot increased, indicatinga greater potential diameter of the shoot. However, final diameterwas dependent on the assimilate supply after bud break. Axillarybuds obviously need a certain developmental stage to be ableto break. When released from correlative inhibition at an earlierstage, increased leaf initiation occurs before bud break.Copyright1994, 1999 Academic Press Age, axillary bud, cell number, cell size, pith, shoot growth, Rosa hybrida, rose     

Canopy development of a determinate and an indeterminate cultivar of Vicia faba L. under contrasting plant distributions and densities

Field experiments were conducted in 1987 and 1988 to quantify differences in canopy formation between an indeterminate and a determinate genotype of Vicia faba L., grown at two plant densities and three spatial distributions. The number of stems per unit area produced by determinate plants was related to the growth rate before flowering. Leaf production per stem per unit of thermal time was similar in both plant types, but twice as many leaves per stem were produced by the indeterminate cultivar. The indeterminate cultivar produced fewer and smaller leaves in the warmer and drier weather of 1988 than in 1987. The determinate genotype produced similar sizes and numbers of leaves in both years, but fewer tillers developed in 1988 than in 1987. Accordingly, leaf mass per unit ground area was greater in 1987 than in 1988 in both genotypes. Except during early flowering, relationships between leaf mass and leaf area were constant, with higher specific leaf areas in the determinate than the indeterminate genotype. Shoot dry matter partitioning into leaves was identical in both years for indeterminate plants, but differed in determinate ones.
It is concluded that canopy development is regulated through individual leaf weight and leaf number per stem in non-tillering indeterminate, and by stem numbers per unit area in tillering determinate plants.     

DIFFERENTIATION OF LATERAL SHOOTS AS THORNS IN ULEX EUROPAEUS

Ulex europaeus is a much-branched shrub with small, narrow, spine-tipped leaves and axillary thorn shoots. The origin and development of axillary shoots was studied as a basis for understanding the changes that occur in the axillary shoot apex as it differentiates into a thorn. Axillary bud primordia are derived from detached portions of the apical meristem of the primary shoot. Bud primordia in the axils of juvenile leaves on seedlings develop as leafy shoots while those in the axils of adult leaves become thorns. A variable degree of vegetative development prior to thorn differentiation is exhibited among these secondary thorn shoots even on the same axis. Commonly the meristems of secondary axillary shoots initiate 3–9 bracteal leaves with tertiary axillary buds before differentiating as thorns. In other cases the meristems develop a greater number of leaves and tertiary buds as thorn differentiation is delayed. The initial stages in the differentiation of secondary shoot meristems as thorns are detected between plastochrons 10–20, depending on vigor of the parent shoot. A study of successive lateral buds on a shoot shows an abrupt conversion from vegetative development to thorn differentiation. The conversion involves the termination of meristematic activity of the apex and cessation of leaf initiation. Within the apex a vertical elongation of cells of the rib meristem initials and their immediate derivatives commences the attenuation of the apex which results in the pointed thorn. All cells of the apex elongate parallel to the axis and proceed to sclerify basipetally. Back of the apex some cortical cells in which cell division has persisted longer differentiate as chlorenchyma. Although no new leaves are initiated during the extension of the apex, provascular strands are present in the thorn tip. Fibrovascular bundles and bundles of cortical fibers not associated with vascular tissue differentiate in the thorn tip and are correlated in position with successive incipient leaves in the expected phyllotactic sequence, the more developed bundles being related to the first incipient leaves. Some secondary shoots displayed variable atypical patterns of meristem differentiation such as abrupt conversion of the apex resulting in sclerification with limited cell elongation and small, inhibited leaves. These observations raise questions concerning the nature of thorn induction and the commitment of meristems to thorns.     

小麦不同蘖位叶片出生的两段线性模式及其品种、播期效应

叶片出生动态是小麦生长发育进程及其协调状况的重要表现,研究发现,小科叶片出生与播后累积ＧＤＤ（ｆｇｒｏｗｉｎｇ ｄｅｇｒｅｅ ｄａｙｓ ａｆｔｅｒ ｓｏｗｉｎｇ）的关系遵循两段（阶段Ⅰ快于阶段Ⅱ）线性模式,护颖分化期为两段模式的分界点,这一规律在正常发育的冬性和春性品种的７主茎及分蘖中表现一致,冬性品种播期１（９月３０日）、播期３（３月２日）的主茎及冬、春性品种各播期的Ｔ３分蘖,因生长发育异常而”